US2354744A - Method of producing shaped resinous artificial materials - Google Patents
Method of producing shaped resinous artificial materials Download PDFInfo
- Publication number
- US2354744A US2354744A US358882A US35888240A US2354744A US 2354744 A US2354744 A US 2354744A US 358882 A US358882 A US 358882A US 35888240 A US35888240 A US 35888240A US 2354744 A US2354744 A US 2354744A
- Authority
- US
- United States
- Prior art keywords
- shaped
- materials
- artificial materials
- producing shaped
- resinous
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title description 6
- 239000012237 artificial material Substances 0.000 title description 3
- 239000000463 material Substances 0.000 description 18
- 239000002904 solvent Substances 0.000 description 15
- 239000000203 mixture Substances 0.000 description 13
- 239000012260 resinous material Substances 0.000 description 10
- 239000000835 fiber Substances 0.000 description 9
- 239000004014 plasticizer Substances 0.000 description 9
- 239000007788 liquid Substances 0.000 description 7
- 229920003023 plastic Polymers 0.000 description 7
- 239000004033 plastic Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 239000010902 straw Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 5
- 229920001290 polyvinyl ester Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 4
- 239000012261 resinous substance Substances 0.000 description 4
- 238000007493 shaping process Methods 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Natural products CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/08—Melt spinning methods
- D01D5/088—Cooling filaments, threads or the like, leaving the spinnerettes
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/16—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of unsaturated carboxylic acids or unsaturated organic esters, e.g. polyacrylic esters, polyvinyl acetate
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/001—Combinations of extrusion moulding with other shaping operations
- B29C48/0018—Combinations of extrusion moulding with other shaping operations combined with shaping by orienting, stretching or shrinking, e.g. film blowing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/05—Filamentary, e.g. strands
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/07—Flat, e.g. panels
- B29C48/08—Flat, e.g. panels flexible, e.g. films
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/21—Nylon
Definitions
- the fusible fibre or film forming resinous substance is reduced to plastic or liquid form either by heating alone or by dissolving it in volatile solvents or plasticizers with or without heating, is then shaped and then immediately or as soon as possible thereafter, is suddenly chilled to temper the same and increase its tenacity or other strength characteristics.
- the artificial materials made by this invention may be of any suitable form.
- they may be filaments of 0.5 to 50 or more denier, which may be'formed into yarns or threads either while in continuous lengths or while in the form of staple fibres.
- They may be in the form of heavier materials such as artificial bristles or horsehair, straw of varying widths of say Vs to 3 inches, wider ribbons, or they may be in the form of foils or films.
- These filaments, bristles, straw or ribbons may be formed by extruding the liquid or plastic material through orifices of proper shape and size, while the foils or films may be formed by casting on the smooth surface of plates, bands or film wheels.
- Articles of heavier form such as may be formed by extruding the material while in plastic or liquid form through an orifice into a mold may also be produced by this invention.
- Any suitable resin may b employed as the fusible film or fibre material.
- these are polyvinyl esters and ethers, e. g. polyvinyl acetate, polyvinyl chloride, polyvinyl-chlor-acetate and copolymers of vinyl acetate and vinyl chloride, polymerized esters of unsaturated acids, e. g. those of the acrylic and methacrylic acid series, fibreor film-forming polyamides, e. g. the products obtained by condensation of diamines with dicarbcxylic or disulphonic acids or by selfcondensation of amino-carboxylic or aminosulphonic acids, and other fibreor film-forming polymers obtainable by condensation of bi-functional reagents.
- polyvinyl esters and ethers e. g. polyvinyl acetate, polyvinyl chloride, polyvinyl-chlor-acetate and copolymers of vinyl acetate and vinyl chloride, polymerized esters of unsaturated
- the material is shaped, it is with cold solid surfaces such as of to 230 subjected to a considerable temperature drop. e. g. of the order of 50 to 200 0., and preferably 100 to 200 C.-when the material is in molten condition prior to shaping, the greater the temperature drop, the stronger the product formed, particularly when it is subjected to a stretching or drawing operation while being formed. In this manner the material may be cooled to a temperature of 0 C. or below.
- the time elapsing between when the material is shaped is preferably very short and to 0.1 or 0.25 second.
- the cooling of the shaped materials may be effected inany suitable-manner. For instance, they may be subjected to a spray of or be immersed in a bath of a liquid that has no appreciable solvent action on the fibre or film forming material and which is cooled to the low temperature required for lowering the temperature of the shaped material to the gree.
- a liquid that has no appreciable solvent action on the fibre or film forming material
- An example of such liquids is brine and other aqueous solutions of salts.
- the cooling may be effected .by means of a blast or current of air or other gas of the requisite low temperature, or by contacting the materials of internally cooled rods, tubes, rollers, plates, etc.
- vents for polyvinyl esters are acetone and ethyl alcohol.
- solvents for polyamides are hot glacial acetic acid, formic acid and phenol. These solvents maybe employed in amounts of 10 to 250% of the weight of the resinous material,
- the plasticizers may be used in amounts of 5 or 10 up to 40% of the weight of the resinous material.
- the temperature at which the composition containing the resinous material may be maintained, prior to shaping may be of the order C. or'more,
- the plasticizers are preferably distributed throughout the resinous material in as uniform a manner as possible. This may be effected by treating the resinous material with a solution or dispersion of the plasticizer in a nonsolvent for the resinous material, allowing the resinous material to absorb the plasticizer from. the solution or dispersion and removing the solvent by evaporation. Another method by which requisite detion or dispersion of the plasticizer in a volatile solvent for the resinous material or by adding the agents to a solution of the resinous material in a volatile solvent. terials are worked, e. g. by malaxation, until the substance is dissolved. when a uniform solution and/or dispersion of the components has been obtained, the volatile solvent may be evaporated, either wholly or in part, so as to leave the required composition.-
- the piasticizer may be removed from the formed materials by extraction with a solvent for the plasticizer, e. g. aqueous alcohol.
- compositions comprising the fusible fibre or -film forming resinous substance that is shaped may also contain other agents in order to modify their properties or to give various effects in the products. They may contain, for example, high boiling solvents, pigments, dyes and/or fire retardants.
- compositions when the compositions contain volatile solvents they may be subjected after extrusion or shaping for a short period of time to heated evaporative atmosphere in order to impart to them sufilcient solidity prior to their being given the chilling treatment.
- the shaped articles may be subjected to various treatments after they have been set, with a view.
- filaments, yarns, bristles, straws and the like they may be subjected to a stretching operation, whether or not they have been stretched before setting.
- a stretching operation applied after setting the materials may be treated with a softening agent, e. g, a solution of a solvent or plasticizer or a solvent vapor, and/or they may be softened by heat.
- a softening agent e. g, a solution of a solvent or plasticizer or a solvent vapor
- the materials especially those having a basis of a fibreor film-forming polymer obtainable by condensation of bifunctional reagents, particularly fibreor film-forming polyamides, are stretched while immersed in or wetted with water or other nonsolvent containing hydroxyl radicles, whether in In the former case the maor while in a steam chamber.
- the tenacity of the products may be still further increased.
- the articles may be subjected to the action of a shrinking agent, e. g. a solution of a solvent for the fibreor filmforming resinous substance, in the absence of liquid or. vapor form.
- a shrinking agent e. g. a solution of a solvent for the fibreor filmforming resinous substance
- they may with advantagebe stretched while immersed in hot water stretching tensionso as further to modify their properties.
- Process for the production of artificial shaped articles comprising shaping a composition comprising a fusible fibre or film forming polyvinyl ester resin'while in a soft and hot condition and immediately thereafter, while the shaped composition. is still in a soft and hot condition, positively causing a drop of to 200 C. in the temperature of said shaped composition in a period of 0.05 to 0.25 second.
- Process for the production .of artificial filaments, threads, bristles or straws comprising extruding a composition comprising a fusible fibre or film forming polyvinyl ester resin while in a soft'and hot condition through an orifice under such conditions as to at least partially solidify the shaped composition and to maintain the same in a soft and hot condition and immediately thereafter, while the shaped composition is still in a soft and hot condition, positively causing a drop of 50-to 200 C. in the temperature of said shaped composition in a period of 0.05 to 0.25 second.
- Process for the production of artificial filaments, threads, bristles or straws comprising extruding a composition comprising a fusible fibre or film forming polyvinyl ester resin while in a soft and hot condition through an orifice under such conditions as to at least partially solidify and to maintain the same in a plastic condition, and immediately thereafter, while the shaped composition is still in a plastic condition, positively cooling the same to a temperature below 0 C. in a period of 0.05 to 0.25 second.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Artificial Filaments (AREA)
Description
Patented Aug. 1, 1944 UNITED STATES PATENT I OFFICE J METHOD OF PRODUCING SHAPED RESIN OUS ARTIFICIAL MATERIALS Camille Dreyfus, New York, N. Y.
No Drawing. Application September 28, 1940,
Serial No. 358,882
3 Claims. (CI. 18-54) materials immediately after their production from molten masses or solutions containing fusible fibre or film forming resinous substances.
Other objects of this invention will appear hereinafter from the following detailed description.
According to my invention the fusible fibre or film forming resinous substance is reduced to plastic or liquid form either by heating alone or by dissolving it in volatile solvents or plasticizers with or without heating, is then shaped and then immediately or as soon as possible thereafter, is suddenly chilled to temper the same and increase its tenacity or other strength characteristics.
The artificial materials made by this invention may be of any suitable form. Thus they may be filaments of 0.5 to 50 or more denier, which may be'formed into yarns or threads either while in continuous lengths or while in the form of staple fibres. They may be in the form of heavier materials such as artificial bristles or horsehair, straw of varying widths of say Vs to 3 inches, wider ribbons, or they may be in the form of foils or films. These filaments, bristles, straw or ribbons may be formed by extruding the liquid or plastic material through orifices of proper shape and size, while the foils or films may be formed by casting on the smooth surface of plates, bands or film wheels. Articles of heavier form such as may be formed by extruding the material while in plastic or liquid form through an orifice into a mold may also be produced by this invention.
Any suitable resin may b employed as the fusible film or fibre material. Examples of these are polyvinyl esters and ethers, e. g. polyvinyl acetate, polyvinyl chloride, polyvinyl-chlor-acetate and copolymers of vinyl acetate and vinyl chloride, polymerized esters of unsaturated acids, e. g. those of the acrylic and methacrylic acid series, fibreor film-forming polyamides, e. g. the products obtained by condensation of diamines with dicarbcxylic or disulphonic acids or by selfcondensation of amino-carboxylic or aminosulphonic acids, and other fibreor film-forming polymers obtainable by condensation of bi-functional reagents. I
Immediately after the material is shaped, it is with cold solid surfaces such as of to 230 subjected to a considerable temperature drop. e. g. of the order of 50 to 200 0., and preferably 100 to 200 C.-when the material is in molten condition prior to shaping, the greater the temperature drop, the stronger the product formed, particularly when it is subjected to a stretching or drawing operation while being formed. In this manner the material may be cooled to a temperature of 0 C. or below. The time elapsing between when the material is shaped is preferably very short and to 0.1 or 0.25 second.
The cooling of the shaped materials may be effected inany suitable-manner. For instance, they may be subjected to a spray of or be immersed in a bath of a liquid that has no appreciable solvent action on the fibre or film forming material and which is cooled to the low temperature required for lowering the temperature of the shaped material to the gree. An example of such liquids is brine and other aqueous solutions of salts. Alternatively the cooling may be effected .by means of a blast or current of air or other gas of the requisite low temperature, or by contacting the materials of internally cooled rods, tubes, rollers, plates, etc.
In case of film or fibre forming resinous materials that melt easily, no plastic inducing substances need be added lbllt they may be used if their effect is desired. With other materials, such substances such as volatile solvents or plasticizers in amounts to render the material more easily reducible to liquid or. plastic form are preferably employed. Examples of volatile soland when it is cooled is of the order of 0.05
vents for polyvinyl esters are acetone and ethyl alcohol. Examples of solvents for polyamides are hot glacial acetic acid, formic acid and phenol. These solvents maybe employed in amounts of 10 to 250% of the weight of the resinous material,
The plasticizers may be used in amounts of 5 or 10 up to 40% of the weight of the resinous material. The temperature at which the composition containing the resinous material may be maintained, prior to shaping may be of the order C. or'more,
When used, the plasticizers are preferably distributed throughout the resinous material in as uniform a manner as possible. This may be effected by treating the resinous material with a solution or dispersion of the plasticizer in a nonsolvent for the resinous material, allowing the resinous material to absorb the plasticizer from. the solution or dispersion and removing the solvent by evaporation. Another method by which requisite detion or dispersion of the plasticizer in a volatile solvent for the resinous material or by adding the agents to a solution of the resinous material in a volatile solvent. terials are worked, e. g. by malaxation, until the substance is dissolved. when a uniform solution and/or dispersion of the components has been obtained, the volatile solvent may be evaporated, either wholly or in part, so as to leave the required composition.-
In the case of the production and treatment of filaments, yarns, bristles, straws and the like,
the piasticizer may be removed from the formed materials by extraction with a solvent for the plasticizer, e. g. aqueous alcohol. a
The compositions comprising the fusible fibre or -film forming resinous substance that is shaped may also contain other agents in order to modify their properties or to give various effects in the products. They may contain, for example, high boiling solvents, pigments, dyes and/or fire retardants.
when the compositions contain volatile solvents they may be subjected after extrusion or shaping for a short period of time to heated evaporative atmosphere in order to impart to them sufilcient solidity prior to their being given the chilling treatment.
The shaped articles may be subjected to various treatments after they have been set, with a view.
to modifying their characteristics. For example, in the case of filaments, yarns, bristles, straws and the like, they may be subjected to a stretching operation, whether or not they have been stretched before setting. Before such a stretching operation applied after setting, the materials may be treated with a softening agent, e. g, a solution of a solvent or plasticizer or a solvent vapor, and/or they may be softened by heat. Advantageousiy, the materials, especially those having a basis of a fibreor film-forming polymer obtainable by condensation of bifunctional reagents, particularly fibreor film-forming polyamides, are stretched while immersed in or wetted with water or other nonsolvent containing hydroxyl radicles, whether in In the former case the maor while in a steam chamber. In this w y. the tenacity of the products may be still further increased.
Alternatively or in addition, the articles may be subjected to the action of a shrinking agent, e. g. a solution of a solvent for the fibreor filmforming resinous substance, in the absence of liquid or. vapor form. Thus they may with advantagebe stretched while immersed in hot water stretching tensionso as further to modify their properties..
It ts to be understood that the foregoing detailed description is merely given by way of i1- lustration and that many variations may be made therein without departing from the spirit of my invention.
Having described my invention, what I desire to secure by Letters Patent is:
1. Process for the production of artificial shaped articles comprising shaping a composition comprising a fusible fibre or film forming polyvinyl ester resin'while in a soft and hot condition and immediately thereafter, while the shaped composition. is still in a soft and hot condition, positively causing a drop of to 200 C. in the temperature of said shaped composition in a period of 0.05 to 0.25 second.
2. Process for the production .of artificial filaments, threads, bristles or straws comprising extruding a composition comprising a fusible fibre or film forming polyvinyl ester resin while in a soft'and hot condition through an orifice under such conditions as to at least partially solidify the shaped composition and to maintain the same in a soft and hot condition and immediately thereafter, while the shaped composition is still in a soft and hot condition, positively causing a drop of 50-to 200 C. in the temperature of said shaped composition in a period of 0.05 to 0.25 second.
3. Process for the production of artificial filaments, threads, bristles or straws comprising extruding a composition comprising a fusible fibre or film forming polyvinyl ester resin while in a soft and hot condition through an orifice under such conditions as to at least partially solidify and to maintain the same in a plastic condition, and immediately thereafter, while the shaped composition is still in a plastic condition, positively cooling the same to a temperature below 0 C. in a period of 0.05 to 0.25 second.
CAMILLE DREYFUB.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US358882A US2354744A (en) | 1940-09-28 | 1940-09-28 | Method of producing shaped resinous artificial materials |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US358882A US2354744A (en) | 1940-09-28 | 1940-09-28 | Method of producing shaped resinous artificial materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2354744A true US2354744A (en) | 1944-08-01 |
Family
ID=23411435
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US358882A Expired - Lifetime US2354744A (en) | 1940-09-28 | 1940-09-28 | Method of producing shaped resinous artificial materials |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2354744A (en) |
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2440190A (en) * | 1944-03-01 | 1948-04-20 | Du Pont | Preparation of nonporous polytetrafluoroethylene articles |
| US2482062A (en) * | 1945-01-19 | 1949-09-13 | Dow Chemical Co | Storage battery separator of polystyrene fiber |
| US2530362A (en) * | 1946-11-22 | 1950-11-14 | Dow Chemical Co | Coagulation of nonelastic polymers |
| US2558730A (en) * | 1947-09-04 | 1951-07-03 | American Cyanamid Co | Method of preparing shaped products from polymers and copolymers of acrylonitrile |
| US2567979A (en) * | 1947-08-05 | 1951-09-18 | Cosmos Dental Products Inc | Dental impression compositions |
| US2567978A (en) * | 1947-08-05 | 1951-09-18 | Cosmos Dental Products Inc | Method of preparing plastic molding compositions |
| US2577915A (en) * | 1948-09-21 | 1951-12-11 | Zd Y Pre Chemicku Vyrobu Narod | Method for producing artificial fibers from high molecular linear polymers or polycondensates respectively |
| US2596128A (en) * | 1949-10-17 | 1952-05-13 | Chavannes Synthetic Fibres Inc | Method and apparatus for producing fine fibers |
| US2695835A (en) * | 1949-12-13 | 1954-11-30 | Du Pont | Process for making rough surfaced filaments |
| US2715763A (en) * | 1950-06-27 | 1955-08-23 | American Viscose Corp | Synthetic textile fiber |
| US2822237A (en) * | 1955-02-21 | 1958-02-04 | Iwamae Hiroshi | Process for producing filament of vinyl chloride polymer |
| US2852143A (en) * | 1956-09-05 | 1958-09-16 | Russell E Taber | Display device |
| US3027602A (en) * | 1957-12-16 | 1962-04-03 | Du Pont | Process for preparing glossy, transparent nylon films by melt extrusion of superpolyamide resins |
| US3226459A (en) * | 1962-10-03 | 1965-12-28 | Union Carbide Corp | Quenching of polyolefin film |
| US3410940A (en) * | 1964-10-12 | 1968-11-12 | Monsanto Co | Mist spinning process |
| US3415922A (en) * | 1965-07-02 | 1968-12-10 | Monsanto Co | Mist spinning |
| US3946094A (en) * | 1972-05-30 | 1976-03-23 | Agency Of Industrial Science & Technology | Method for manufacturing filaments of crystalline plastics thereof |
| US4797424A (en) * | 1988-02-19 | 1989-01-10 | Abt Nancy G | Saline solution for frozen foam |
| WO1996041907A1 (en) * | 1995-06-08 | 1996-12-27 | Wacker-Chemie Gmbh | Fusible, chlorine-free vinyl acetate copolymer fibre |
| US6045592A (en) * | 1998-09-08 | 2000-04-04 | Leanne Paquin | Method and kit for dyeing shaped nylon plastics |
-
1940
- 1940-09-28 US US358882A patent/US2354744A/en not_active Expired - Lifetime
Cited By (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2440190A (en) * | 1944-03-01 | 1948-04-20 | Du Pont | Preparation of nonporous polytetrafluoroethylene articles |
| US2482062A (en) * | 1945-01-19 | 1949-09-13 | Dow Chemical Co | Storage battery separator of polystyrene fiber |
| US2530362A (en) * | 1946-11-22 | 1950-11-14 | Dow Chemical Co | Coagulation of nonelastic polymers |
| US2567979A (en) * | 1947-08-05 | 1951-09-18 | Cosmos Dental Products Inc | Dental impression compositions |
| US2567978A (en) * | 1947-08-05 | 1951-09-18 | Cosmos Dental Products Inc | Method of preparing plastic molding compositions |
| US2558730A (en) * | 1947-09-04 | 1951-07-03 | American Cyanamid Co | Method of preparing shaped products from polymers and copolymers of acrylonitrile |
| US2577915A (en) * | 1948-09-21 | 1951-12-11 | Zd Y Pre Chemicku Vyrobu Narod | Method for producing artificial fibers from high molecular linear polymers or polycondensates respectively |
| US2596128A (en) * | 1949-10-17 | 1952-05-13 | Chavannes Synthetic Fibres Inc | Method and apparatus for producing fine fibers |
| US2695835A (en) * | 1949-12-13 | 1954-11-30 | Du Pont | Process for making rough surfaced filaments |
| US2715763A (en) * | 1950-06-27 | 1955-08-23 | American Viscose Corp | Synthetic textile fiber |
| US2822237A (en) * | 1955-02-21 | 1958-02-04 | Iwamae Hiroshi | Process for producing filament of vinyl chloride polymer |
| US2852143A (en) * | 1956-09-05 | 1958-09-16 | Russell E Taber | Display device |
| US3027602A (en) * | 1957-12-16 | 1962-04-03 | Du Pont | Process for preparing glossy, transparent nylon films by melt extrusion of superpolyamide resins |
| US3226459A (en) * | 1962-10-03 | 1965-12-28 | Union Carbide Corp | Quenching of polyolefin film |
| US3410940A (en) * | 1964-10-12 | 1968-11-12 | Monsanto Co | Mist spinning process |
| US3415922A (en) * | 1965-07-02 | 1968-12-10 | Monsanto Co | Mist spinning |
| US3946094A (en) * | 1972-05-30 | 1976-03-23 | Agency Of Industrial Science & Technology | Method for manufacturing filaments of crystalline plastics thereof |
| US4797424A (en) * | 1988-02-19 | 1989-01-10 | Abt Nancy G | Saline solution for frozen foam |
| WO1996041907A1 (en) * | 1995-06-08 | 1996-12-27 | Wacker-Chemie Gmbh | Fusible, chlorine-free vinyl acetate copolymer fibre |
| US5880239A (en) * | 1995-06-08 | 1999-03-09 | Wacker-Chemie Gmbh | Fusible chlorine-free vinyl acetate copolymer fibres |
| RU2142524C1 (en) * | 1995-06-08 | 1999-12-10 | Вакер-Хеми ГмбХ | Meltable chlorine-free fiber from vinyl acetate copolymer |
| CN1070545C (en) * | 1995-06-08 | 2001-09-05 | 瓦克化学有限公司 | Fusible Chlorine-Free Vinyl Acetate Copolymer Fiber |
| US6045592A (en) * | 1998-09-08 | 2000-04-04 | Leanne Paquin | Method and kit for dyeing shaped nylon plastics |
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